Grownsy BC023
Grownsy BC023 is a nasal aspirator (FDA Class II; FDA product code KDQ, Bottle, Collection, Vacuum) made by Oak Tech LLC, listed in FDA GUDID since 28 Apr 2024 (UDI-DI 00860011589501), registry data as of 22 Oct 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00860011589501 | Date28 Apr 2024 | StatusListed |
Official records
- AccessGUDID record 00860011589501
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Grownsy
- Generic name
- Nasal aspirator, electric
- Model / reference
- BC023
- Primary DI / UDI-DI
- 00860011589501
- FDA product code
- KDQ
- GMDN term
- Nasal aspirator, electric
- Device class
- Class II
- Regulation number
- 880.6740
- GUDID distribution status
- In Commercial Distribution
Similar devices
Other devices filed under FDA product code KDQ (Bottle, Collection, Vacuum).
- PLEUR-EVAC CHEST DRAINAGE SYSTEMS by Deknatel, Inc.
- ARGYLE SUCTION CANISTER W/DISP. LINER by Sherwood Medical Co.
- Thora-Vent Thoracic Vent TVOCP by Uresil Corp.
- THORA-KLEX 350 ML PEDIATRIC CHEST DRAINAGE SYSTEM by Davol Inc.
- Vide ST423-0001 by Alleva Medical Limited
- Vide ST422-0001 by Alleva Medical Limited
- THORAX-KLEX CHEST DRAINAGE UNIT by C. R. Bard, Inc.
- Thora-Vent Thoracic Vent TV11-13 by Uresil Corp.
- VACUUM SUCTION FILTER by K & G Healthcare Ind., Inc.
- Baleen NBPT520 by US Endoscopy